Gold Nanorods Incorporated Cathode for Better Performance of Polymer Solar Cells

Mahmoud, Alaa Y.; Izquierdo, Ricardo; Truong, Vo-Van

doi:https://doi.org/10.1155/2014/464160

Journal of Nanomaterials

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Abstract Introduction Results and Discussion Conclusion Acknowledgments References Copyright Related Articles

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Energy Conversion and Storage: Synthesis, Mechanism, and Applications of Nanomaterials

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Research Article | Open Access

Volume 2014 | Article ID 464160 | https://doi.org/10.1155/2014/464160

Gold Nanorods Incorporated Cathode for Better Performance of Polymer Solar Cells

Alaa Y. Mahmoud,^1,2,3Ricardo Izquierdo,²and Vo-Van Truong¹

Academic Editor: Ji Sun Im

Received26 Sept 2013

Revised21 Nov 2013

Accepted21 Nov 2013

Published29 Jan 2014

Abstract

The effect of inserting low density of gold nanorods in the metallic rear electrode of polymer solar cells on their performance was studied. Gold nanorods were introduced by spin-coating their aqueous solution directly on top of the poly(3-hexylthiophene-2,5-diyl):[6,6]-phenyl-C₆₁-butyric-acid-methyl-ester layer. The resulting devices showed a 5% increase in the short circuit current that leads to a 14% enhancement in the power conversion efficiency. Investigation on the photocurrent spectral response of devices with/without gold nanorods revealed that incorporating the rods helped in enhancing the devices photogenerated current near the plasmonic absorption modes of the rods. The enhancement in the devices efficiency is related to the increase in their absorptivity due to the far-field and near-field effect of localized surface plasmon resonance induced by the presence of the rods in the interface between the photoactive layer and the metallic rear electrode.

1. Introduction

Intensive research has been dedicated to enhancing the power conversion efficiency (PCE) of organic solar cells (OSCs) due to their attractive features such as solvent solubility, portability, flexibility, and low cost, [1–4]. Up to now, the PCE of bulk heterojunction (BHJ) polymer solar cells made by the blend of the polymer poly(3-hexylthiophene-2,5-diyl) (P3HT) and the fullerene-derivative -phenyl-C₆₁-butyric-acid-methyl-ester (PCBM) has reached ~5% [5]. Unlike their inorganic counterparts, the absorption of light in organic materials creates bounded electron-hole pairs (excitons) with a short diffusion length rather than the free charge carriers. Thereby, the photoactive layer in OSCs has to be in the range of a few hundred nanometers of thickness to limit the recombination of the charge carriers. Such thin photoactive film allows for more transmission loss of the incident light [2, 4].

To overcome the absorption loss in thin-film photovoltaic (PV) devices, the optical path length of the incident light inside the absorber has to be enlarged without increasing the absorber thickness [6–8]. This could be achieved by utilizing the light trapping mechanism associated with excited plasmonic particles. Plasmonic phenomenon in illuminated metallic nanoparticles (MNPs), such as gold and silver MNPs, occurs when the oscillations of the incident electric field resonate with the ones of the electronic charge in the surface of MNPs. Such resonance allows MNPs to absorb light in the visible region of the spectra, leading to intensification, by a factor of 100, in the electromagnetic (EM) field surrounding them [5]. Metallic nanoparticles are widely used in thin-film solar cells to enhance their absorption of light by utilizing the far-field and near-field effect associated with their localized surface plasmon resonance (LSPR) [9–15].

Although various shapes of gold nanoparticles support the LSPR, the scattering cross-section of particles with a cylindrical shape, however, is much larger than the one associated with the spherical particles [16]. This motivated the use of the rod shape of gold nanoparticles in the current work. In previous works we investigated the effect of inserting gold nanorods (Au NRs) into P3HT:PCBM BHJ-OSCs by depositing them on the anodic layer, indium tin oxide (ITO) [17], or by mixing them either with the anodic buffer layer [14] or the photoactive one [18].

In spite of the fact that the fraction of the backward scattered light into the cell (from MNPs placed on the cell’s rear electrode) is comparable to the forward scattered one (from MNPs placed on the front electrode), it has been reported that placing the MNPs on the cell’s rear electrode is preferable to having them in the front one [19]. This is due to the fact that the loss in the absorption of light at wavelengths with energies higher than the energy of surface plasmon is prevented by limiting the destructive interference between the scattered and unscattered light, while light at lower energy gets coupled inside the cell [6, 19, 20]. Furthermore, placing the particles in contact with the photoactive layer makes it possible for the intensified EM field around them to reach the photoactive film and excite more charge carriers. In addition, MNPs in the photoactive layer introduce quenching energy states for the excitons, which reduces the number of free charges carriers that are collected by electrodes [11, 12, 18]. These points suggested that having the Au NRs on top of the photoactive layer would lead to better increases in both EM field and the optical path length of the incident light inside the absorber. In addition, there have been no previous studies on the effect of depositing MNPs in contact with the polymer solar cell’s cathode.

In the this study, we report on the effect of incorporating gold nanorods into the rear electrode of BHJ-OSCs on their overall performance by spin-coating many layers of Au NRs directly on top of the P3HT:PCBM film. The investigation on the spectral response of the resulting photogenerated current from devices with/without Au NRs revealed that the photogenerated current for devices incorporating Au NRs was enhanced near the plasmonic absorption modes of the rods. The presence of Au NRs on top of P3HT:PCBM layer would induce more trapping and intensification of the incident EM in the photoactive layer. This thereby will enhance the film absorptivity to the incident light, leading to improved overall performance of the devices.

2. Experimental Methods

Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) (CLEVIOS P VP AI 4083) was purchased from HC Stark. P3HT with a high regioregularity (98%) and an average molecular weight <50,000 MW was purchased from Rieke Metals. PCBM (>99.5%) and 1,2-dichlorobenzene (anhydrous, 99%) were purchased from Sigma-Aldrich. The materials were used as received without further purification.

Gold nanorods in an aqueous solution were obtained from the Institut National de la Recherche Scientifique at Varennes (INRS-EMT). Details about preparation of Au NRs were mentioned in [17]. The concentration of Au NRs in the aqueous solution was ~1.593 10¹² rods/mL. Figure 1 shows the transmission electron microscopy (TEM) image of the rods, which reveals that the ratio between rods’ long and short axes is around 4.

For device fabrication, the P3HT:PCBM blends at a 1 : 0.8 ratio were prepared inside a nitrogen-filled glovebox by separately dissolving 20 mg of P3HT and 16 mg of PCBM in 1 mL of 1,2-dichlorobenzene. Equal volumes of P3HT and PCBM solutions were then mixed together and stirred overnight at room temperature to ensure more homogeneity. Prepatterned/cleaned ITO-coated glass substrates were subjected to an oxygen plasma treatment before spin-coating PEDOT:PSS solution after passing it through a 0.45 μm PVDF filter. The ITO/PEDOT:PSS substrates were baked at 120°C for 1 h and then transferred to the nitrogen-filled glovebox for the deposition of the photoactive layer. The photoactive film P3HT:PCBM was spin-coated on top of the modified ITO/PEDOT:PSS electrodes after being passed through a 0.45 μm PTFE filter. Substrates were then left to dry in a covered petri dish for 30 min. Afterwards, various Au NRs layers (1, 3, and 5) were directly spin-coated on top of the photoactive film. The spin-coating of Au NRs was performed using a two-step process, first at a slow speed of 200 RPM for 3 sec and then at 1000 RPM for 10 sec. Substrates were then annealed at 150°C for 30 min to be dehydrated. The device fabrication was completed by evaporating a LiF/Al bilayer cathode under pressure less than torr to yield substrates with devices having an active area of 0.16 cm²/each. The final configuration of the Au NRs incorporated device is presented in Figure 2 along with the chemical formulas of both P3HT and PCBM materials.

(a)

(b)

3. Characterizations

OSC devices were characterized under ambient condition without any encapsulation, in which they were placed underneath the UV solar simulator lamp (xenon lamp,Oriel Instruments) that was equipped with AM 1.5 G filer. The output intensity of the lamp was adjusted to 100 mW/cm² using a silicon photodiode (LI-200 Pyranometer). The current-voltage measurements were carried out using a source-meter (Keithley 2400). The PV parameters, open circuit voltage (), short circuit current (), fill factor (FF), and PCE, were measured in devices with and without Au NRs that were made under the same experimental conditions. Since our devices were exposed to air at a certain point during evaporation and characterization processes, the values of PCE were generally low. For analyzing data and scientific visualization solution, the Qtiplot program was used in which the error bars were determined.

The photocurrent spectral response measurements of the devices were carried out by varying the wavelengths of the incident light from 400 nm to 800 nm using a Newport 74000 monochromator.

The optical properties of both Au NRs and P3HT:PCBM were studied using a UV-Vis spectrophotometer (PerkinElmer LAMBDA 650 spectrophotometer). The surface structure of the resulting Au NRs layers was characterized using a scanning electron microscopy (FEG-SEM Hitachi S-4700), in which the density of the rods in the layer was determined.

4. Results and Discussion

Figure 3 illustrates the normalized absorption spectra for Au NRs solution along with the spectra of the P3HT:PCBM film. The blue curve for Au NRs solution shows two peaks of their resonance modes, transverse and longitudinal, respectively, located at 540 nm and 740 nm. The red curve shows that the absorption of the P3HT:PCBM photoactive film ranges from 370 nm to 650 nm, with an absorbance maximum around 518 nm and two shoulder peaks around 560 and 610 nm. This absorbance profile is due to the π-π* electronic transitions between 0-1 and 0-0 spin states for the maximum and the shoulder peaks, respectively [21, 22]. It is clear that the position of the transverse absorption peak of the rods is associated with the absorption maximum of the P3HT:PCBM film. Besides, the longitudinal absorption peak of the rods is close to the IR absorption edge of the photoactive film. Hence, the intensified EM field around Au NRs would increase the absorption of the photoactive film near the plasmon peaks of the rods, in which an enhancement in the film absorption near the IR region is expected [14, 18].

To compare both of the microscopic and spectroscopic properties of the deposited Au NRs layers, one, three, and five layers of Au NRs were separately spin-coated on ITO-coated glass. The SEM images in Figure 4 show that such spin-coating deposition of many layers of Au NRs produced rods with various densities and arbitrary alignments on the substrate. Accordingly, the spectral measurements of the obtained 1, 3, and 5 rods layer(s), illustrated in Figure 5, were different. The presence of Au NRs with different alignments at the ITO surface explains the appearance of the two peaks in the spectrum. A more intense peak is observed for the five-layer deposit, which produced denser rods in the layer (~4 10⁹ cm⁻²). For one and three layers of rods, the particles densities were ~8 10⁸ and , respectively.

To examine the effect of incorporating Au NRs on top of the photoactive layer of the OSC devices, the PV parameters of fully fabricated devices with/without rods were measured and compared. Figure 6 illustrates the curves under illumination and in dark conditions for reference device along with devices incorporated Au NRs on top of the photoactive layer, and Table 1 summarizes their corresponding PV parameters. As Table 1 shows, depositing the Au NRs on top of the P3HT:PCBM film increased the by up to 5% which succeeded in enhancing the PCE by up to 14.1% for devices incorporating one layer of Au NRs. However, devices with 3 and 5 layers of the rods on top of the photoactive layer showed a slight decrease in the PCE. The increase in the device performance via incorporating a layer of the rods in contact with the cell’s back electrodes could be explained by the following mechanisms: the EM field associated with the LSPR of Au NRs (near-field effect) was intensified near the photoactive layer, or the optical path length of the incident light inside the photoactive layer was increased due to the backward scattering (far-field effect) of the incident light [5, 6, 19]. Both mechanisms will result in intensification of the incident light inside the P3HT:PCBM layer, leading to better generation of the charge carriers in the photoactive layer. This would cause the increase in the and the enhancement in the PCE of the resulting device.

(a)

(b)

Figure 7(a) shows the spectral measurements of the photogenerated current density for reference device along with the one that incorporated a layer of Au NRs on top of the photoactive film. The photocurrent measurements give a picture of the photogenerated charge carriers upon light illumination [20]. It is obvious that the was enhanced by the deposition of the rods layer. To study the effect of the multimodes excitation of the nanorods on the photogenerated current density before () and after () incorporating one layer of Au NRs on the cell’s rear electrode, we investigated in Figure 7(b) the spectral measurements of the ratio / along with the spectrum of Au NRs solution. Since the absorption of our photoactive film does not exceed 650 nm, there was a decrease in the enhancement of the photogenerated current around 680–760 nm. As Figure 7(b) depicts, the enhanced by 1.13-, 1.14-, and 1.16-folds, respectively, at 460, 640, and 670 nm. These remarkable enhancements in the are near the transverse absorption mode of the Au NRs and the tail of the longitudinal one, respectively, considering the probability of shifting the absorption maxima for Au NRs with changing the surrounding environments. The increase in the could be related to the increase in the generated free charge carriers in the photoactive film due to the backward scattering process from the rods, or the intensification of the EM field surrounding them. Although there was no large enhancement in the absorption profile of the P3HT:PCBM/AuNRs films near the IR region, a very small increase in the was observed at this region, particularly at 670–700 nm, which can be attributed to the longitudinal absorption mode of Au NRs. Hence, we suggested that the photogeneration of excitons near the transverse and longitudinal absorption modes of Au NRs was enhanced, which improved the total device efficiency. Our results are somewhat similar to those obtained by Chen et al. [15] who reported on enhancements in organic cells with gold nanofilms thermally evaporated in vacuum onto a LiF/Al electrode. Their results showed an enhancement in the / ratio near the absorption profile of nanotextured Au thin films.

(a)

(b)

For more than a layer of the rods on the P3HT:PCBM film,3- and 5-layer cases, as presented in Table 1, there was a reduction in the values of both and PCE as compared to the corresponding ones in the reference device. Since these devices have denser rods on top of the photoactive film with arbitrary orientations, the possibility of having some rods embedded in the photoactive film is increased. Hence, we would expect that the photogenerated excitons near the P3HT:PCBM/AuNRs interface to be subjected to recombination, which in turn lowered the numbers of free charge carriers that reached the electrodes in these cases, thus reducing both and PCE [23].

Table 1 also reveals that the devices series resistance () was increased from 10.5 to 22.5 Ωcm² with having more than a layer of Au NRs deposited on top of the photoactive film. The increase in led to a reduction in the FF from ~63% to 56%. The increase and decrease in both and FF, respectively, affected the overall performance of the resulting device. Since Au NRs were dispersed in an aqueous solution, we suggest that having more than a layer of Au NRs on top of the photoactive film will accelerate the diffusion of oxygen and water into the photoactive layer, which resulted in the device degradation. The increase in the devices could be considered as an evidence for the degradation of the photoactive film [24]. This degradation would be another reason for the reduction in the device performance with more than a layer of the rods on top of the photoactive film.

5. Conclusion

We achieved ~14% and 5% increase, respectively, in power conversion efficiency and short circuit current density of polymer solar cells by spin-coating a layer of Au NRs on top of the photoactive film in contact with the cell’s rear electrode. The improvement in the device performance was related to both far-field and near-field effect associated with the LSPR of Au NRs. The spectral measurements of the short circuit current revealed that its values were increased near the plasmonic absorption modes of the rods. More than a layer of Au NRs (3- and 5-layer cases) on top of the photoactive film, however, decreased the overall performance of the resulting devices. We found that dense Au NRs in the layer increased the devices series resistance by up to 12.5%. Such increase in the series resistance would be considered as an evidence for the degradation of the photoactive layer, which negatively affected both devices’ short circuit current and power conversion efficiency.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of the paper.

Acknowledgments

Alaa Y. Mahmoud acknowledges with thanks Dr. Dongling Ma from INRS-EMT for providing the gold nanorods and Dr. Muthukumaran Packirisamy for access to his laboratory. This work was supported by the Natural Sciences and Engineering Research Council of Canada.

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Copyright

Copyright © 2014 Alaa Y. Mahmoud et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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